Review
Copyright ©The Author(s) 2023.
World J Diabetes. Feb 15, 2023; 14(2): 62-75
Published online Feb 15, 2023. doi: 10.4239/wjd.v14.i2.62
Table 1 Protective effects of caffeic acid and derivatives in diabetes and associated complications
Type of study/condition
Dose
Mode of action
Ref.
STZ-induced diabetic miceTopical administration of propolis at 20 μLHealing of human DFU[79]
CAPE at 5 μmol/kg and 10 μmol/kgIncreased wound contraction and re-epithelialization by reducing oxidative stress[80,81]
Diabetic mice with DFUTopical application of propolisStimulated VEGF and activated NO/cGMP pathway[82,83]
Diabetic mice with renal damageCA at 5%Decreased AGEs, IL-1b, and IL-6, and reduced activity of renal AR and SDH.[92]
STZ-induced diabetic mice, nephropathyCA at 10-50 mg/kgModulation of autophagy pathway[93]
CA at 40 mg/kg Improved renal parameters, and downregulated the expression of miR-636[94]
CAPE and CAPE-pNO2 at 20 μmol/kg/dInhibited inflammation through the Akt/NF-κB pathway and prevented renal fibrosis through the TGF-β/Smad pathway[95]
Diabetes induced in HUVECsCAPE treatment at 3-10 μMReduced VEGF-induced angiogenesis[96]
STZ-induced diabetic rats, retinopathyCAF6 and CAF12 at 250 mMModulation of ERK1/2 and protein kinase-B/Akt signaling pathways[98]
STZ-induced diabetic rats, neuropathyCAPE at 10 μM/kg/dInhibition of iNOS enzyme[102]
Alloxan-induced diabetic mice, CVDCA at 50 mg/kgReduced atherogenic indices such as TG, LDL-c, VLDL-c, and TC[53]
CA at 2%Improved glycemic control and lipid metabolism, increased plasma antithrombin-III and protein C activities, and decreased MDA, IL-β, IL-6, and TNF-α levels[34]
STZ-induced T1D rat model, CVDCAPA at 3 and 15 mg/kgReduced myocardial infarction and amelioration of cardiac dysfunction[103]